GM21640
Fibroblast from Skin, Unspecified
Description:
EHLERS-DANLOS SYNDROME, TYPE I; EDS1
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Heritable Diseases |
Biopsy Source
|
Unspecified
|
Cell Type
|
Fibroblast
|
Tissue Type
|
Skin
|
Transformant
|
Untransformed
|
Sample Source
|
Fibroblast from Skin, Unspecified
|
Family Member
|
1
|
Relation to Proband
|
proband
|
Confirmation
|
Molecular characterization before cell line submission to CCR
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
PDL at Freeze |
6.65 |
Passage Frozen |
2 |
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin confirmed by LINE assay |
|
Remarks |
Clinically affected; negative collagen I and III studies; iliac arterial dissection; several family members with aneurysms; affected brother is GM22034; joint pain; joint swelling in ankles; prominent forehead; epicanthal fold; malar hypoplasia; soft auricles; abnormal ear canals; micrognathia; wide palate; SM cleft; blue sclerae; pectus carinatum; pain and tenderness in abdomen; left and right carotid bruit; soft hyperextensible skin; cigarette paper and keliod scarring; easy bruising; piezogenic papules; hyperextension in shoulders, elbows, hips, knees and CMC, MCP, PIP and DIP joints; pes planus; genu valga; chokes in sleep; visual floaters; headaches; rib pain; urinary tract infections; mild disc disease at C4-C7; grade I spondylolisthesis in L5-S1 lumbar spine; disc extrusion at L4-S1; see GM21639 Lymphoid; molecular analysis of this donor subject with respect to the COL5A1 gene showed one allele as wild type and one allele with a G>A change in exon 52 (null allele) |
Cumulative PDL at Freeze |
6.65 |
Passage Frozen |
2 |
Split Ratio |
1:3 |
Temperature |
37 C |
Percent CO2 |
5% |
Percent O2 |
AMBIENT |
Medium |
Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent |
Serum |
15% fetal bovine serum Not inactivated |
Substrate |
None specified |
Supplement |
- |
|
|